Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Expanded cord blood progenitors refer to a class of cellular therapies where hematopoietic stem and progenitor cells (HSPCs) derived from umbilical cord blood are expanded ex vivo to increase the total cell dose prior to transplantation. The specific product described in the context (dilanubicel; DVX-101) is an off-the-shelf, non-HLA-matched, cryopreserved progenitor cell product developed using a proprietary Notch-mediated expansion platform. By culturing purified CD34+ cells with the Notch ligand Delta-1, the manufacturing process generates a high dose of myeloid progenitors. When infused as an adjuvant to a conventional cord blood transplant, these cells provide a rapid, transient wave of myeloid reconstitution (neutrophils and monocytes), effectively bridging the period of profound neutropenia typically associated with cord blood grafts. This approach aims to reduce the time to engraftment and the risk of early transplant-related mortality (TRM) and infections in patients with high-risk hematologic malignancies.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on expanded cord blood progenitors.